Identify the product of the following reaction:
Benzene diazonium halide
Nitro benzene
Sodium benzoate
Benzene halide
To determine the product of the reaction, we need to analyze the nature of the chemical reaction involved. The reaction in question pertains to the chemistry of benzene and its derivatives, particularly involving the transformation of primary aromatic amines into diazonium salts.
In general, when an aromatic amine such as aniline (C₆H₅NH₂) is treated with nitrous acid (HNO₂, usually generated in situ from sodium nitrite (NaNO₂) and a mineral acid like HCl), the primary product is a diazonium salt. This reaction is conducted at low temperatures, typically 0-5°C, to prevent further decomposition of the diazonium compound.
The equation representing this process is as follows:
C₆H₅NH₂ + HNO₂ + HX → C₆H₅N₂⁺X⁻ + 2H₂O
Here, C₆H₅N₂⁺X⁻
is the benzene diazonium halide, where X
represents a halide ion derived from the mineral acid used (such as chloride, bromide, etc.).
This diazonium salt is a crucial intermediate in the synthesis of various aromatic compounds, used in dye and pigment formation.
Based on this fundamental understanding of the reaction mechanism, the correct product formed is the benzene diazonium halide.
Correct Answer: Benzene diazonium halide
SN1 reaction mechanism takes place by following three steps –
The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group (which generally consists of halide groups or other electron-withdrawing groups) with a nucleophile in a given organic compound.
The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:
The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.